Canonical Allele Identifier: CA365377053

Gene: CCN6

Linked Data

• gnomAD v4: 6-112069605-G-C
• MyVariant Identifiers: chr6:g.112390808G>C (hg19) ; chr6:g.112069605G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069605G>C , CM000668.2:g.112069605G>C	GRCh38
NC_000006.11:g.112390808G>C , CM000668.1:g.112390808G>C	GRCh37
NC_000006.10:g.112497501G>C	NCBI36
NG_011748.1:g.20531G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.1050G>C MANE Select	ENSP00000357655.4:p.Glu350Asp
ENST00000639360.1:c.951G>C	ENSP00000491774.1:p.Glu317Asp
ENST00000230529.9:c.1050G>C	ENSP00000230529.5:p.Glu350Asp
ENST00000361714.5:c.1050G>C	ENSP00000354734.2:p.Glu350Asp
ENST00000368663.4:c.*356G>C	ENSP00000357652.4:n.*356G>C
ENST00000368664.7:c.*454G>C	ENSP00000357653.3:n.*454G>C
ENST00000368666.6:c.1104G>C	ENSP00000357655.3:p.Glu368Asp
ENST00000409166.5:c.378G>C	ENSP00000386467.1:p.Glu126Asp
ENST00000454589.5:c.*454G>C	ENSP00000395928.1:n.*454G>C
ENST00000604763.5:c.1050G>C	ENSP00000473777.1:p.Glu350Asp
ENST00000613648.1:n.885G>C
ENST00000620524.3:n.981G>C
NM_003880.3:c.1050G>C	NP_003871.1:p.Glu350Asp
NM_198239.1:c.1104G>C	NP_937882.1:p.Glu368Asp
NR_125353.1:n.1304G>C
NR_125354.1:n.1224G>C
XM_011536220.1:c.1050G>C	XP_011534522.1:p.Glu350Asp
XM_011536221.1:c.*454G>C	XP_011534523.1:n.*454G>C
XM_011536223.1:c.468G>C	XP_011534525.1:p.Glu156Asp
XM_011536223.3:c.468G>C	XP_011534525.1:p.Glu156Asp
XR_001743705.1:n.1652G>C
NM_003880.4:c.1050G>C	NP_003871.1:p.Glu350Asp
NM_198239.2:c.1050G>C MANE Select	NP_937882.2:p.Glu350Asp
NR_125353.2:n.1368G>C
NR_125354.3:n.1195G>C